ID: 130067689 | ATAC-STARR-seq lymphoblastoid silent region 13886 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45672137..45672466) | | |
ID: 130067688 | ATAC-STARR-seq lymphoblastoid silent region 13885 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45671757..45671806) | | |
ID: 130067687 | ATAC-STARR-seq lymphoblastoid silent region 13884 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45671507..45671696) | | |
ID: 130067686 | ATAC-STARR-seq lymphoblastoid silent region 13883 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45645968..45646037) | | |
ID: 130067685 | ATAC-STARR-seq lymphoblastoid silent region 13882 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45645668..45645957) | | |
ID: 130067684 | ATAC-STARR-seq lymphoblastoid active region 19228 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45553847..45553956) | | |
ID: 127896735 | H3K4me1 hESC enhancer GRCh37_chr22:46044567-46045067 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45648687..45649187) | | |
ID: 127896734 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:45997202-45997774 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45601322..45601894) | | |
ID: 126863166 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr22:46021696-46022895 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45625816..45627015) | | |
ID: 112695105 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr22:46034441-46035640 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45638561..45640158) | | |
ID: 112695104 | Sharpr-MPRA regulatory region 3085 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45627589..45627883) | | |
ID: 106480077 | RNA, U6 small nuclear 1161, pseudogene [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45624531..45624632, complement) | | |
ID: 105373069 | uncharacterized LOC105373069 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45635981..45656656) | | |
ID: 105373068 | uncharacterized LOC105373068 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45647554..45656696, complement) | | |
ID: 105373067 | uncharacterized LOC105373067 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45636615..45640429, complement) | | |
ID: 100506737 | long intergenic non-protein coding RNA 1589 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45604432..45605647, complement) | TCONS_00029353 | |
ID: 57088 | phospholipid scramblase 4 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (146192335..146251105, complement) | TRA1 | 607612 |
ID: 25814 | ataxin 10 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45671834..45845307) | ATX10, E46L, HUMEEP, SCA10 | 611150 |
ID: 6280 | S100 calcium binding protein A9 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (153357854..153361023) | 60B8AG, CAGB, CFAG, CGLB, L1AG, LIAG, MAC387, MIF, MRP14, NIF, P14, S100-A9 | 123886 |
ID: 6279 | S100 calcium binding protein A8 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (153390032..153422583, complement) | 60B8AG, CAGA, CFAG, CGLA, CP-10, L1Ag, MA387, MIF, MRP8, NIF, P8, S100-A8 | 123885 |